Team:Warsaw/Calendar-Main/31 July 2008
From 2008.igem.org
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1. Marker<br> | 1. Marker<br> | ||
2. pellet negative control<br> | 2. pellet negative control<br> | ||
- | 3. supernatant negative | + | 3. supernatant negative control<br> |
4. pellet 37°C 0.1 mM IPTG <br> | 4. pellet 37°C 0.1 mM IPTG <br> | ||
5. supernatant 37°C 0.1 mM IPTG<br> | 5. supernatant 37°C 0.1 mM IPTG<br> |
Revision as of 16:10, 24 October 2008
Purification of proteins: Z-alpha and Z-omegaPiotr, Emilia
Cloning of omega_A DNA fragment to pACYC177+OmpA_alphaMichał K.
Cloning of truncated fragment of protein AMichał K.The arrow shows place of our overexpressed protein: 1. 22°C 0.5 mM IPTG 2. 22°C 0.1 mM IPTG 3. 22°C 1 mM IPTG 4. Marker 5. negative control 6. 37°C 0.1 mM IPTG 7. 37°C 0.5 mM IPTG 8. 37°C 1 mM IPTG Fig. 2. Pellets and supernatants from Z-alpha induction with various IPTG concentrations The arrow shows place of our overexpressed protein: 1. Marker 2. pellet negative control 3. supernatant negative control 4. pellet 37°C 0.1 mM IPTG 5. supernatant 37°C 0.1 mM IPTG 6. sonicate 22°C 0.1 mM IPTG 7. sonicate 22°C 0.5 mM IPTG 8. pellet 37°C 0.5 mM IPTG 9. supernatant 37°C 0.5 mM IPTG
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